Brintidox 10 mg/ml + 5 mg/ml Ögondroppar, suspension

Quốc gia: Thụy Điển

Ngôn ngữ: Tiếng Thụy Điển

Nguồn: Läkemedelsverket (Medical Products Agency)

Thành phần hoạt chất:

brinzolamid; timololmaleat

Sẵn có từ:

DOC Generici Srl

Mã ATC:

S01ED51

INN (Tên quốc tế):

brinzolamide; timololmaleat

Liều dùng:

10 mg/ml + 5 mg/ml

Dạng dược phẩm:

Ögondroppar, suspension

Thành phần:

mannitol Hjälpämne; brinzolamid 10 mg Aktiv substans; bensalkoniumklorid Hjälpämne; timololmaleat 6,83 mg Aktiv substans

Loại thuốc theo toa:

Receptbelagt

Tóm tắt sản phẩm:

Förpacknings: Droppbehållare, 3 x 5 ml; Droppbehållare, 6 x 5 ml; Droppbehållare, 5 ml

Tình trạng ủy quyền:

Godkänd

Ngày ủy quyền:

2020-02-24

Đặc tính sản phẩm

1
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Brintidox 10 mg/mL + 5 mg/mL eye drops, suspension
_ _
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One ml of suspension contains 10 mg brinzolamide and timolol maleate
corresponding to 5 mg
timolol.
Excipient with known effect:
One ml of suspension contains 0.10 mg benzalkonium chloride.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Eye drops, suspension (eye drops)
White to off-white uniform suspension, pH 7.2 (approximately).
_ _
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Decrease of intraocular pressure (IOP) in adult patients with
open-angle glaucoma or ocular
hypertension for whom monotherapy provides insufficient IOP reduction
(see section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
Use in adults, including the elderly
The dose is one drop of /.../ in the conjunctival sac of the affected
eye(s) twice daily.
When using nasolacrimal occlusion or closing the eyelids, the systemic
absorption is reduced. This
may result in a decrease in systemic side effects and an increase in
local activity (see section 4.4).
If a dose is missed, treatment should be continued with the next dose
as planned. The dose should not
exceed one drop in the affected eye (s) twice daily.
When substituting another ophthalmic antiglaucoma medicinal product
with /.../, the other medicinal
product should be discontinued and /.../ should be started the
following day.
Special populations
_Paediatric population _
The safety and efficacy of /.../ in children and adolescents aged 0 to
18 years have not yet been
established. No data are available.
_Hepatic and renal impairment _
No studies have been conducted with /.../ or with timolol 5 mg/ml eye
drops in patients with hepatic
or renal impairment. No dosage adjustment is necessary in patients
with hepatic impairment or in
patients with mild to moderate renal impairment.
3
/.../ has not been studied in patients with severe renal impairment
(creatinine clearance <30 ml/min) or
in